GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Ac3H11_1694 in Cupriavidus basilensis 4G11

Align ABC transporter ATP-binding protein (characterized, see rationale)
to candidate RR42_RS29445 RR42_RS29445 ABC transporter permease

Query= uniprot:A0A165KER0
         (358 letters)



>FitnessBrowser__Cup4G11:RR42_RS29445
          Length = 358

 Score =  155 bits (392), Expect = 2e-42
 Identities = 101/331 (30%), Positives = 172/331 (51%), Gaps = 38/331 (11%)

Query: 15  LLVLPLILQSFGNAWVRIADLALLYVLLALGLNIVVGYAGLLDLGYVAFYAVGAYLFALM 74
           LL+ P    S+   W+      L+Y +  LGL ++ GY GLL +G+ AF  VGAY  A +
Sbjct: 32  LLIAPGWASSY---WIAQLGFVLIYAIAGLGLMVLSGYTGLLSIGHAAFLGVGAYTQAWL 88

Query: 75  ASPHLADNFAAFAAMFPNGLHTSLWIVIPVAALLAAFFGAMLGAPTLKLRGDYLAIVTLG 134
            S H      A  A                AA L+A  G ++G P L+++G YLAI TL 
Sbjct: 89  TS-HGVPFVPALLA----------------AAALSALTGVVVGLPALRVKGIYLAIATLA 131

Query: 135 FGEIIRIFLNNLDHPVNLTNGPKGLGQIDSVKVFGLDLGKRLEVFGFDINSVTLYYYLFL 194
           FG I+   L   +   ++T G  GL                 +++G+ ++    +YYL L
Sbjct: 132 FGLIVEEILARWE---SVTGGNAGLPVAAP------------QLWGYVLDGPVAFYYLSL 176

Query: 195 VLVVVSVIICYRLQDSRIGRAWMAIREDEIAAKAMGINTRNMKLLAFGMGASFGGVSGAM 254
            + +++ +    L  S  GRA++AIR+ EI+A++MGI+    K L+F + A+  G++GA+
Sbjct: 177 AVCLLATLAVLNLLRSATGRAFIAIRDSEISAQSMGIHLARYKTLSFALSAALVGIAGAL 236

Query: 255 FGAFQGFVSPESFSLMESVMIVAMVVLGGIGHIPGVILGAVLLSALPEVLRYVAGPLQAM 314
           +     ++SPE F + +S+ ++ +VV+GG+G + G  LGA+ L  +P+++  +A  L   
Sbjct: 237 YAHKLRYISPEQFGIAQSIDLLLLVVVGGLGSVHGAFLGAIFLIVMPQMI-VLAKDLLPP 295

Query: 315 TDGRLDSAILRQLLIALAMIIIMLLRPRGLW 345
             G+     ++ L+  L ++  +L  P GL+
Sbjct: 296 AIGQASG--MQALVYGLVLMAFVLFEPMGLY 324


Lambda     K      H
   0.328    0.144    0.430 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 298
Number of extensions: 13
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 358
Length of database: 358
Length adjustment: 29
Effective length of query: 329
Effective length of database: 329
Effective search space:   108241
Effective search space used:   108241
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.7 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory